Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426711Generated: November 3, 2026

Sodium hydride → HCID 67397564, compound

https://huagongshe.com/reaction/1426711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
Reactant3-Cyanobenzene-1-sulfonyl chlorideHCID 2801360—
ReactantHCID 67397020HCID 67397020—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67397564HCID 6739756481%

Reaction Steps

To a suspension of sodium hydride (60% in oil, 60 mg) in tetrahydrofuran (5 mL) were added dropwise a solution (5 mL) of tert-butyl {[5-(2-cyanopyridin-3-yl)-4-fluoro-1H-pyrrol-3-yl]methyl}methylcarbamate (330 mg) in tetrahydrofuran, 15-crown-5 (330 mg) and 3-cyanobenzenesulfonyl chloride (302 mg) under ice-cooling and the mixture was stirred for 15 min. The reaction mixture was diluted with water, and extracted with ethyl acetate. The separated aqueous layer was extracted again with ethyl acetate. The combined organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=6:1→2:1) to give the title compound as a pale-yellow oil (yield 401 mg, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-9a98b0f5e8984ea6ab87dc5accda0114
Source noteuspto-grants-2015_01